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首页> 外文期刊>Malaria Journal >Global proteomic analysis of plasma from mice infected with Plasmodium berghei ANKA using two dimensional gel electrophoresis and matrix assisted laser desorption ionization-time of flight mass spectrometry
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Global proteomic analysis of plasma from mice infected with Plasmodium berghei ANKA using two dimensional gel electrophoresis and matrix assisted laser desorption ionization-time of flight mass spectrometry

机译:使用二维凝胶电泳和基质辅助激光解吸电离飞行时间质谱对感染伯氏疟原虫ANKA的小鼠血浆进行整体蛋白质组学分析

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Background A global proteomic strategy was used to identify proteins, which are differentially expressed in the murine model of severe malaria in the hope of facilitating future development of novel diagnostic, disease monitoring and treatment strategies. Methods Mice (4-week-old CD1 male mice) were infected with Plasmodium berghei ANKA strain, and infection allowed to establish until a parasitaemia of 30% was attained. Total plasma and albumin depleted plasma samples from infected and control (non-infected) mice were separated by two-dimensional gel electrophoresis (2-DE). After staining, the gels were imaged and differential protein expression patterns were interrogated using image analysis software. Spots of interest were then digested using trypsin and the proteins identified using matrix-assisted laser desorption and ionization-time of flight (MALDI-TOF) mass spectrometry (MS) and peptide mass fingerprinting software. Results Master gels of control and infected mice, and the corresponding albumin depleted fractions exhibited distinctly different 2D patterns comparing control and infected plasma, respectively. A wide range of proteins demonstrated altered expression including; acute inflammatory proteins, transporters, binding proteins, protease inhibitors, enzymes, cytokines, hormones, and channel/receptor-derived proteins. Conclusions Malaria-infection in mice results in a wide perturbation of the host serum proteome involving a range of proteins and functions. Of particular interest is the increased secretion of anti-inflammatory and anti apoptotic proteins.
机译:背景技术全球蛋白质组学策略被用于鉴定在严重疟疾的鼠模型中差异表达的蛋白质,以希望促进新型诊断,疾病监测和治疗策略的未来发展。方法用伯氏疟原虫ANKA株感染小鼠(4周龄CD1雄性小鼠),并建立感染直至获得30%的寄生虫血症。通过二维凝胶电泳(2-DE)分离感染和对照(未感染)小鼠的总血浆和白蛋白消耗血浆样品。染色后,对凝胶成像,并使用图像分析软件询问差异蛋白表达模式。然后使用胰蛋白酶消化感兴趣的斑点,并使用基质辅助激光解吸和电离飞行时间质谱(MS)和肽质量指纹软件对蛋白质进行鉴定。结果对照小鼠和感染小鼠的主凝胶以及相应的白蛋白耗竭部分分别显示出与对照血浆和感染血浆相比不同的2D模式。多种蛋白质表现出改变的表达,包括;急性炎症蛋白,转运蛋白,结合蛋白,蛋白酶抑制剂,酶,细胞因子,激素和通道/受体衍生蛋白。结论小鼠中的疟疾感染导致宿主血清蛋白质组受到广泛干扰,其中涉及多种蛋白质和功能。特别令人感兴趣的是抗炎和抗凋亡蛋白的分泌增加。

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